Glu | |
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Salts [] | |
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Glutamic acid hydrochloride | |
Molecular structure via molpic | |
Conformer structure via 3Dmol.js | |
Molecular formula | C5H9NO4[1] |
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Molecular mass | 147.13 g/mol[1] |
Predicted LogP | -3.7[1] |
Chirality | racemic[2] |
Identifiers [] | |
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IUPAC name | 2-aminopentanedioic acid[1] |
SMILES | C(CC(=O)O)C(C(=O)O)N[1] |
InChI | InChI=1S/C5H9NO4/c6-3(5(9)10)1-2-4(7)8/h3H,1-2,6H2,(H,7,8)(H,9,10)[1] |
InChIKey | WHUUTDBJXJRKMK-UHFFFAOYSA-N[1] |
Dosing |
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Glutamic acid
(Redirected from D-Glutamic acid)
Glutamic acid (also known as DL-Glutamic acid, Glutamic acid DL-form, 4-04-00-03028, Glutamic acid, dl-(ii), Glutamic acid, dl-[ii], Glutamic acid, dl, Glutamic acid DLform, 2-azaniumyl-5-hydroxy-5-oxopentanoate, Glutaminsaeure or H-DL-Glu-OH) is a substance of the amino acid class.
Chemistry
Glutamic acid is typically found in the form of its hydrochloride salt.
Stereochemistry
DL-Glutamic acid is a racemic mixture of the logical stereoisomers:
Stereoisomers [] |
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See also
External links
- Glutamic acid (Wikipedia)
- Glutamic acid / D-Glutamic acid / L-Glutamic acid (Wikidata)
- Glutamic acid / D-Glutamic acid / L-Glutamic acid (PubChem)
- Glutamic acid / D-Glutamic acid / L-Glutamic acid (ChEMBL)
- Glutamic acid / D-Glutamic acid / L-Glutamic acid (ChEBI)
- Glutamic acid / D-Glutamic acid / L-Glutamic acid (Common Chemistry)
- Glutamic acid / D-Glutamic acid / L-Glutamic acid (HMDB)
- Glutamic acid / D-Glutamic acid / L-Glutamic acid (KEGG)
- Glutamic acid / D-Glutamic acid / L-Glutamic acid (UNII)
- Glutamic acid / D-Glutamic acid / L-Glutamic acid (EPA DSSTox)